食物剥夺型肥胖(fa/fa) Zucker大鼠脑和垂体促肾上腺皮质激素释放激素结合蛋白。

E Timofeeva, Y Deshaies, F Picard, D Richard
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引用次数: 6

摘要

本研究旨在验证肥胖和食物剥夺等实验条件是否可以改变大鼠大脑中促肾上腺皮质激素释放激素(CRH)结合蛋白(BP)的表达,从而促进食物摄入,减少产热。采用原位杂交、组织化学和免疫组织化学方法,对任意喂食、剥夺食物24小时、剥夺食物24小时、再喂食6小时的瘦Zucker大鼠和肥胖Zucker大鼠中CRH-BP的表达进行了评估。在瘦Zucker大鼠和肥胖Zucker大鼠中,剥夺食物导致体重减轻,并伴有血浆皮质酮水平的可逆升高。食物剥夺和肥胖(在较小程度上)诱导CRH-BP mRNA在内侧视前区(MPOA)背侧的表达。对CRH-BP有免疫反应的神经元MPOA背侧的出现证实了食物剥夺导致的CRH-BP基因的诱导。食物剥夺(特别是)和肥胖也增加了基底外侧杏仁核(BLA)中CRH-BP mRNA的水平。CRH-BP在MPOA和BLA中表达的增强在食物剥夺后被重新喂食逆转。In lean Fa/?大鼠垂体细胞中CRH-BP mRNA水平在剥夺食物后显著降低,再摄食后恢复。当随意提供食物时,瘦大鼠垂体前叶表达CRH-BP的细胞数量明显高于肥胖大鼠。禁食24 h后,瘦大鼠垂体表达CRH-BP的细胞数量显著减少。总之,目前的结果表明,食物剥夺和肥胖(在较小程度上)可以选择性地影响CRH-BP的表达。考虑到CRH- bp对CRH系统的失活作用,以及MPOA和BLA在CRH产热和厌食作用中的潜在作用,我们可以认为,在肥胖和食物剥夺后,CRH- bp基因的诱导是一种减少能量消耗和刺激食物摄入的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Corticotropin-releasing hormone-binding protein in brain and pituitary of food-deprived obese (fa/fa) Zucker rats.

The present study was conducted to verify whether experimental conditions such as obesity and food deprivation, which promote food intake and reduce thermogenesis, could modify the expression of the corticotropin-releasing hormone (CRH)-binding protein (BP) in the rat brain. In situ hybridization, histochemistry, and immunohistochemistry were used to assess the expression of CRH-BP in lean (Fa/?) and obese (fa/fa) Zucker rats that were fed ad libitum, food deprived for 24 h, or food deprived for 24 h and refed for 6 h. In both lean and obese rats, food deprivation led to a reduction in body weight that was accompanied by a reversible increase in plasma corticosterone levels. Food deprivation and, to a lesser degree, obesity induced the expression of CRH-BP mRNA in the dorsal part of the medial preoptic area (MPOA). This induction of the CRH-BP gene led to by food deprivation was confirmed by the appearance in the dorsal part of the MPOA of neurons immunoreactive to CRH-BP. Food deprivation (in particular) and obesity also increased the levels of CRH-BP mRNA in the basolateral amygdala (BLA). The enhanced CRH-BP expression in the MPOA and BLA in response to food deprivation was reversed by refeeding. In lean Fa/? rats, the CRH-BP mRNA level in the pituitary cells was significantly decreased after food deprivation and restored after refeeding. When food was provided ad libitum, the number of cells expressing CRH-BP in the anterior pituitary was significantly higher in lean rats than in obese animals. Food deprivation for 24 h decreased dramatically the number of pituitary cells expressing CRH-BP in lean rats. Altogether, the present results demonstrate that food deprivation and, to a lesser extent, obesity can selectively affect the expression of CRH-BP. Given both the inactivating effect of CRH-BP on the CRH system and the potential roles played by the MPOA and BLA in the thermogenic and anorectic effects of CRH, it can be argued that the induction of the CRH-BP gene in obesity and after food deprivation occurs as a mechanism to reduce energy expenditure and to stimulate food intake.

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